A New Generation of T7 RNA Polymerase-Independent Inducible Expression Plasmids for Trypanosoma brucei 英文参考文献.docVIP
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A New Generation of T7 RNA Polymerase-Independent Inducible Expression Plasmids for Trypanosoma brucei 英文参考文献
ANewGenerationofT7RNAPolymerase-Independent
InducibleExpressionPlasmidsforTrypanosomabrucei
JackSunter1,BillWickstead2,3,KeithGull3,MarkCarrington1*
1DepartmentofBiochemistry,UniversityofCambridge,Cambridge,UnitedKingdom,2CentreforGeneticsandGenomics,UniversityofNottingham,Nottingham,United
Kingdom,3SirWilliamDunnSchoolofPathology,UniversityofOxford,Oxford,UnitedKingdom
Abstract
ExpressionoftransgenesiscentraltoforwardandreversegeneticanalysisinTrypanosomabrucei.Theinducibleexpression
of transgenes in trypanosomes is based on the tetracycline repressor binding to a tetracycline operator to prevent
transcriptionintheabsenceoftetracycline.Thesameinduciblesystemisusedtoproducedouble-strandedRNAforRNAi
knockdown of target genes. This study describes a new plasmid pSPR2.1 that drives consistent high-level expression of
tetracyclinerepressorinprocyclicformtrypanosomes.Acomplementaryexpressionplasmid,p3227,wasconstructed.The
major difference between this and current plasmids is the separation of the inducible transgene and selectable marker
promotersbytheplasmidbackbone.Theplasmidp3227wasabletosupportinducibleexpressionincelllinescontaining
pSPR2.1aswellastheestablishedLister42729-13cellline.p3666,aderivativeofp3227,wasmadeforinducibleexpression
of stem loop RNAi constructs and was effective for knockdown of DRBD3,which hadproved problematic using existing
RNAiplasmidswithhead-to-headpromoters.Theplasmidsystemwasalsoabletosupportinducibletransgeneexpression
andDRBD3RNAiknockdowninbloodstreamformcellsexpressingtetracyclinerepressor fromanintegratedcopyofthe
plasmidpHD1313.
Citation: Sunter J, Wickstead B, Gull K, Carrington M (2012) A New Generation of T7 RNA Polymerase-Independent Inducible Expression Plasmids for
Trypanosomabrucei.PLoSONE7(4):e35167.doi:10.1371/journal.pone.0035167
Editor:AshokAiyar,LouisianaStateUniversityHealthSciencesCenter,UnitedStatesofAmerica
ReceivedDecember19,2011;AcceptedMarch13,2012;PublishedApril12,2012
Copyright: ? 2012 Sunter et al. This
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